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Chirality Sensing and Size Discrimination of Anions by Macrotricyclic Cyclen–Disodium Complexes**
Two macrotricyclic ligands composed of two face-to-face octadentate metal chelates were synthesized. These cage-shaped disodium complexes had special recognition ability for various counter anions. Specific chiral dicarboxylates bound to the complexes within the cavity and exhibited chirality induct...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280822/ http://dx.doi.org/10.1002/open.201402049 |
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author | Ito, Hiroshi Shinoda, Satoshi |
author_facet | Ito, Hiroshi Shinoda, Satoshi |
author_sort | Ito, Hiroshi |
collection | PubMed |
description | Two macrotricyclic ligands composed of two face-to-face octadentate metal chelates were synthesized. These cage-shaped disodium complexes had special recognition ability for various counter anions. Specific chiral dicarboxylates bound to the complexes within the cavity and exhibited chirality induction properties. For instance, N-Boc-Asp dianion strongly induced circular dichroism (CD) signals, but N-Boc-Glu dianion, which is one carbon longer, did not. |
format | Online Article Text |
id | pubmed-4280822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42808222015-01-02 Chirality Sensing and Size Discrimination of Anions by Macrotricyclic Cyclen–Disodium Complexes** Ito, Hiroshi Shinoda, Satoshi ChemistryOpen Communications Two macrotricyclic ligands composed of two face-to-face octadentate metal chelates were synthesized. These cage-shaped disodium complexes had special recognition ability for various counter anions. Specific chiral dicarboxylates bound to the complexes within the cavity and exhibited chirality induction properties. For instance, N-Boc-Asp dianion strongly induced circular dichroism (CD) signals, but N-Boc-Glu dianion, which is one carbon longer, did not. Blackwell Publishing Ltd 2014-12 2014-09-17 /pmc/articles/PMC4280822/ http://dx.doi.org/10.1002/open.201402049 Text en © 2014 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Communications Ito, Hiroshi Shinoda, Satoshi Chirality Sensing and Size Discrimination of Anions by Macrotricyclic Cyclen–Disodium Complexes** |
title | Chirality Sensing and Size Discrimination of Anions by Macrotricyclic Cyclen–Disodium Complexes** |
title_full | Chirality Sensing and Size Discrimination of Anions by Macrotricyclic Cyclen–Disodium Complexes** |
title_fullStr | Chirality Sensing and Size Discrimination of Anions by Macrotricyclic Cyclen–Disodium Complexes** |
title_full_unstemmed | Chirality Sensing and Size Discrimination of Anions by Macrotricyclic Cyclen–Disodium Complexes** |
title_short | Chirality Sensing and Size Discrimination of Anions by Macrotricyclic Cyclen–Disodium Complexes** |
title_sort | chirality sensing and size discrimination of anions by macrotricyclic cyclen–disodium complexes** |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280822/ http://dx.doi.org/10.1002/open.201402049 |
work_keys_str_mv | AT itohiroshi chiralitysensingandsizediscriminationofanionsbymacrotricycliccyclendisodiumcomplexes AT shinodasatoshi chiralitysensingandsizediscriminationofanionsbymacrotricycliccyclendisodiumcomplexes |